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Carboxylic acids epoxidation

Sodium borohydride is a mild and selective reducing reagent. In ethanol solution it reduces aldehydes and ketones rapidly at 25°C, esters very slowly, and is inert toward functional groups that are readily reduced by lithium aluminum hydride carboxylic acids, epoxides, lactones, nitro groups, nitriles, azides, amides, and acid chlorides. [Pg.475]

BUTOXYETHYL ACETATE or BUTOXYETHYL CELLOSOLVE ACETATE [Union Carbide] (112-07-2) CsH.,03 Combustible liquid. Forms explosive mixture with air [explosion limits in air (vol %) 0.9 to 8.5 flash point 160°F/71°C autoignition temp 645°F/341°C Fire Rating 2]. Violent reaction on contact with strong oxidizers. Incompatible with alkali metals carboxylic acids epoxides such as glycidol, isocyanates, permanganates, peroxides and hydroperoxides, ammonium persulfate ... [Pg.173]

Copolymer Formation by Carboxylic Acid + Epoxide Reaction... [Pg.371]

Table 5.32. Block copolymer formation in PA/PEST blends by carboxylic acid + epoxide coupling agent... Table 5.32. Block copolymer formation in PA/PEST blends by carboxylic acid + epoxide coupling agent...
Table 5.9 PA/PEST blends - blends containing a coupling agent copolymer formation by carboxylic acid + epoxide reaction ... Table 5.9 PA/PEST blends - blends containing a coupling agent copolymer formation by carboxylic acid + epoxide reaction ...
See other pages where Carboxylic acids epoxidation is mentioned: [Pg.398]    [Pg.6]    [Pg.186]    [Pg.295]    [Pg.449]    [Pg.469]    [Pg.476]    [Pg.477]    [Pg.528]    [Pg.541]    [Pg.543]    [Pg.552]    [Pg.564]    [Pg.568]    [Pg.577]    [Pg.592]    [Pg.594]    [Pg.611]    [Pg.671]    [Pg.672]    [Pg.672]    [Pg.728]    [Pg.794]    [Pg.822]    [Pg.845]    [Pg.886]    [Pg.887]    [Pg.887]    [Pg.887]    [Pg.915]    [Pg.921]    [Pg.921]    [Pg.922]    [Pg.1040]    [Pg.1045]    [Pg.1058]    [Pg.347]    [Pg.376]    [Pg.531]   
See also in sourсe #XX -- [ Pg.235 ]



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Carboxylation epoxide

Epoxidation acids

Epoxides acids

Epoxides carboxylates

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